New indication: Pneumococcal 13-valent conjugate vaccine (Prevnar 13) was granted accelerated FDA marketing approval for the prevention of pneumonia and invasive disease (infection of blood or spinal fluid) caused by Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F in adults age 50 years and older.
On December 30, 2011, pneumococcal 13-valent conjugate vaccine (Prevnar 13) was granted accelerated FDA marketing approval for the prevention of pneumonia and invasive disease (infection of blood or spinal fluid) caused by Streptococcus pneumoniae serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F in adults age 50 years and older. Prevnar 13 was previously approved for use in children aged 6 weeks through 5 years for the prevention of invasive disease caused by 13 different serotypes of S. pneumoniae and for the prevention of otitis media caused by 7 of the serotypes of the bacterium.
Efficacy. Prevnar 13's efficacy was established in five phase 3, noninferiority, clinical trials conducted in the United States and Europe, evaluating the immunogenicity of Prevnar 13 in individuals who were either previously vaccinated or unvaccinated with Pneumovax 23. In all 5 studies, antibody levels elicited by Prevnar 13 were similar or higher to those elicited by the comparator for the 12 serotypes common to both vaccines. Antibody responses to Prevnar 13 were lower in subjects >65 years of age compared to antibody responses in subjects between ages 50 and 59 years. Of note, there have been no controlled trials in adults demonstrating a decrease in pneumonia or invasive disease after vaccination with Prevnar 13. Moreover, the effectiveness of Prevnar 13 when administered <5 years after Pneumovax 23 is not currently known.
Safety. The safety of Prevnar 13 was evaluated in 6 controlled studies conducted in the United States and Europe (n=6,198) in patients aged 50 to 95 years. In these studies, the most commonly reported adverse reactions were pain at the injection site, fatigue, headache, muscle pain, joint pain, decreased appetite, injection-site redness, injection-site swelling, limitation of arm movement, chills, and rash.
David Calabrese of OptumRx Talks Top Three Drugs in Pipeline, Industry Trends in Q2
July 1st 2020In this week's episode of Tuning Into The C-Suite podcast, MHE's Briana Contreras chatted with David Calabrese, R.Ph, MHP, who is senior vice president and chief pharmacy officer of pharmacy care services company, OptumRx. David is also a member of Managed Healthcare Executives’ Editorial Advisory Board. During the discussion, he shared the OptumRx Quarter 2 Drug Pipeline Insights Report of 2020. Some of the information shared includes the three notable drugs currently being reviewed or those that have been recently approved by the FDA. Also discussed were any interesting industry trends to watch for.
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